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1352731-59-9

Br(1-)*C53H72NO2(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352731-59-9 Structure

  • Basic information

    1. Product Name: Br(1-)*C53H72NO2(1+)
    2. Synonyms: Br(1-)*C53H72NO2(1+)
    3. CAS NO:1352731-59-9
    4. Molecular Formula:
    5. Molecular Weight: 835.064
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352731-59-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Br(1-)*C53H72NO2(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Br(1-)*C53H72NO2(1+)(1352731-59-9)
    11. EPA Substance Registry System: Br(1-)*C53H72NO2(1+)(1352731-59-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1352731-59-9(Hazardous Substances Data)

1352731-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352731-59-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,7,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352731-59:
(9*1)+(8*3)+(7*5)+(6*2)+(5*7)+(4*3)+(3*1)+(2*5)+(1*9)=149
149 % 10 = 9
So 1352731-59-9 is a valid CAS Registry Number.

1352731-59-9Downstream Products

1352731-59-9Relevant articles and documents

Design, synthesis, and application of tartaric acid derived N-spiro quaternary ammonium salts as chiral phase-transfer catalysts

Waser, Mario,Gratzer, Katharina,Herchl, Richard,Mueller, Norbert

, p. 251 - 254 (2012/02/06)

A novel class of tartaric acid-derived N-spiro quaternary ammonium salts was synthesised starting from known TADDOLs. These compounds were found to catalyse the asymmetric α-alkylation of glycine Schiff bases with high enantioselectivities and in good yie

Investigations concerning the syntheses of TADDOL-derived secondary amines and their use to access novel chiral organocatalysts

Gratzer, Katharina,Waser, Mario

, p. 3661 - 3670 (2013/02/22)

A structurally carefully diversified library of novel TADDOL-derived chiral secondary amines was synthesized and investigated for their applicability to obtain new organocatalysts like chiral Lewis bases and chiral phase-transfer catalysts. The scope and limitations of the developed syntheses routes to access these catalysts as well their catalytic performance in different benchmark reactions were systematically investigated. The most powerful of the catalysts prepared was found to be highly useful for the phase-transfer catalyzed α-alkylation of glycine Schiff base (high yields and up to 93% ee). Georg Thieme Verlag KG Stuttgart · New York.

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